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首页> 外文期刊>International journal of antimicrobial agents >Plasma and cerebrospinal fluid concentrations oflinezolid in neurosurgical critically ill patients with proven or suspected central nervous system infections
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Plasma and cerebrospinal fluid concentrations oflinezolid in neurosurgical critically ill patients with proven or suspected central nervous system infections

机译:患有确诊或疑似中枢神经系统感染的神经外科重症患者的利奈唑胺血浆和脑脊液浓度

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Linezolid is a valuable treatment option for central nervous system (CNS) infections caused by multidrug-resistant Gram-positive micro-organisms. Data regarding its penetration into the CNS have shown wide variability. The aim of this study was to describe the population pharmacokinetics of linezolid in plasma and cerebrospinal fluid (CSF) in critically ill patients with external CSF drainage and proven or suspected CNS infections. This was an observational pharmacokinetic (PK) study in 11 critically ill patients with proven or suspected CNS infection receiving linezolid. Serial blood and CSF samples were taken and were subject to population PK analysis. The median (interquartile range) of AUC_(0-12h) was 47.6 (17.9-58.6) mgh/L in plasma and 21.1 (18.8-30.4) mgh/L in CSF, with a median CSF/plasma ratio of 0.77. At pre-dose at steady state, a strong positive correlation was observed between linezolid concentrations in CSF and plasma (Spearman's rho = 0.758; P= 0.011). For a minimum inhibitory concentration (MIC) of 2 mg/L, the median AUC_(0-24h)/MIC values in plasma and CSF were <80 in all patients. A three-compartment linear model was found to be most appropriate. The mean value for linezolid clearance was 16.6 L/h and mean volume of distribution was 101.3 L. No covariate relationships could be supported on any of the parameters. Linezolid demonstrated good penetration into the CNS but high interindividual PK variability. Administration of higher than standard doses of linezolid and therapeutic drug monitoring should therefore be considered as options to optimise linezolid dosing in critically ill patients with CNS infections.
机译:利奈唑胺是由多重耐药性革兰氏阳性微生物引起的中枢神经系统(CNS)感染的宝贵治疗选择。关于其渗透到中枢神经系统的数据显示出很大的可变性。这项研究的目的是描述利奈唑胺在血浆和脑脊液(CSF)的血浆药物和脑脊液(CSF)的人群药代动力学,这些患者患有外部CSF引流并被证实或怀疑患有CNS感染。这是一项观察性药代动力学(PK)研究,研究对象是11例接受利奈唑胺确诊或怀疑中枢神经系统感染的重症患者。采集系列血液和脑脊液样本,并进行种群PK分析。血浆中AUC_(0-12h)的中位数(四分位数范围)为47.6(17.9-58.6)mgh / L,CSF中为21.1(18.8-30.4)mgh / L,CSF /血浆中位数比为0.77。在稳定的服药前,观察到脑脊液中利奈唑胺浓度与血浆之间存在强正相关(Spearman Rh = 0.758; P = 0.011)。对于2 mg / L的最低抑菌浓度(MIC),所有患者的血浆和CSF中AUC_(0-24h)/ MIC的中值均小于80。发现三室线性模型是最合适的。利奈唑胺清除率的平均值是16.6 L / h,平均分布体积是101.3L。任何参数都不能支持协变量关系。利奈唑胺显示出良好的渗透入中枢神经系统,但个体间PK变异性高。因此,应考虑给予高于标准剂量的利奈唑胺和监测治疗药物,作为优化中枢神经系统感染重症患者利奈唑胺剂量的选择。

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